Structural variants detected by the 10x Genomics Long Ranger pipeline.

Table reflects SVs identified by 10x Long Range pipelines applied to 10x reads aligned to the GRCh38 reference sequence in the eight selected regions (Table 1). Columns show the region, GRCh38 chromosome, position and identifier of the SV, followed by the GRCh38 allele and the alternate allele. The last column reflects detailed information including SV type (deletion or insertion) and length, as output by the Long Ranger pipeline. (TSV)